Description
New Build Biologics facility based in Dublin have a CONTRACT requirement for an experienced C&Q Engineer to complete the final commissioning, qualification & validation stages of this 'nearing completion project'!We are looking for experienced and hands-on CQV Engineers who are able to get the project complete and qualified prior to handover to the client - equipment experience within the Biopharmaceutical sector is essential and we are looking for candidates to work with equipment such as: Purification equipment (filtration/chromatography) OR Fermentors/Bioreactors/Buffer Hold vessels etc.
You will be responsible for driving the field execution, IOC, IOC and final reports.
Role and responsibilities:
- Liaise with CQV start-up team in relation to punch list closure both pre-mechanical completion and during the CQV execution phase.
- Ensure Commissioning readiness of all Systems to support Equipment Start-up and IOQ Testing.
- CQV interface with EIDA/or Master Project Database equivalent system, ensure full traceability at all times for all LSCC systems.
- Liaise with CQV Document Generation Lead in relation to generation and approval of; DQ/Design Reviews/SLIA/Test Matrices/Risk Assessments/QA Vendor Assessments/FAT/SAT/CTP/IOQ Protocols.
- Execution of all LSCC CQV deliverables; IOQ, field execution.
- Ensure timely approval of all Commissioning and IOQ Final Report.
Call me for further information on this role - START ASAP!
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